Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04186169 · ClinicalTrials.gov registry record · NA

Peri-Atrial Inflammatory Fat and Atrial Fibrillation

A NA study, sponsored by Johns Hopkins University.

Terminated
Registry status
NA
Development phase
4
Enrollment target

NCT04186169: Clinical Trial NA study, sponsored by Johns Hopkins University.

NCT04186169 is a NA study that was terminated before completion, run by Johns Hopkins University. The registered enrollment target is 4 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT04186169, a NA study, was terminated before completion, sponsored by Johns Hopkins University.

TERMINATED
Registry status
NA
Development phase
4 participants
Enrollment target

Study Summary

Atrial fibrillation (AF) impacts the lives of 30 million people worldwide. Pulmonary vein isolation (PVI) by catheter ablation is effective for paroxysmal AF, but the success rate remains marginal at 60-80%. For persistent AF, defined as continuous AF that sustains longer than 7 days, the success rate is even lower. The low success rate of AF ablation reflects the fact that there is no effective target identified to modify the underlying substrate beyond PVI. Recently, investigators have made an exciting discovery that higher mean CT attenuation values of peri-atrial fat tissue, correlated with inflammatory fat, are associated with higher incidence of recurrence after AF ablation. In this protocol, investigators will investigate the clinical significance of peri-atrial inflammatory fat tissue in AF using ultra-high resolution CT.

Primary Outcome

Freedom from any documented episode of AF lasting longer than 30 seconds after the performance of a single ablation procedure without the use of antiarrhythmic drugs (AADs). No episode of AF occurring within the initial 3-month blanking period after ablation will be counted. An episode of AF will be considered part of the primary outcome analyses if it lasts longer than 30 seconds and is documented by any form of monitoring, regardless of symptoms. A repeat left atrial (LA) ablation procedure at

Interventions

  • PROCEDURE Catheter ablation

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2021-02-19
Est. Completion 2024-11-12
Phase NA
Johns Hopkins University

1,448 total trials

Why NCT04186169 stopped before completion

NCT04186169 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Catheter ablation is the first listed.

NCT04186169 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04186169 about?

NCT04186169 is a clinical study titled "Peri-Atrial Inflammatory Fat and Atrial Fibrillation". Atrial fibrillation (AF) impacts the lives of 30 million people worldwide. Pulmonary vein isolation (PVI) by catheter ablation is effective for paroxysmal AF, but the success rate remains marginal at 60-80%. For persistent AF, defined as continuous AF that sustains longer than 7 days, the success ra...

What is the current status of trial NCT04186169?

This trial is currently terminated. It is a NA study. The enrollment target is 4 participants. The study started on 2021-02-19. Estimated completion is 2024-11-12.

What interventions are being tested in trial NCT04186169?

The interventions under investigation include: Catheter ablation (PROCEDURE).

Who is sponsoring clinical trial NCT04186169?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04186169's enrollment target sits among peer trials

4 1996th of 2000 higher than 5 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04186169, the US trial registry maintained by the National Library of Medicine. NCT04186169 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.